Canonical Allele Identifier: CA2341531000
Gene: FPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746524T= , CM000681.2:g.51746524T= GRCh38
NC_000019.9:g.52249777T= , CM000681.1:g.52249777T= GRCh37
NC_000019.8:g.56941589T= NCBI36
NG_023426.1:g.10374A= , LRG_146:g.10374A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.471A= ENSP00000470750.2:p.Thr157=
ENST00000600815.2:c.471A= ENSP00000472936.2:p.Thr157=
ENST00000304748.5:c.471A= MANE Select ENSP00000302707.3:p.Thr157=
ENST00000304748.4:c.471A= ENSP00000302707.3:p.Thr157=
ENST00000595042.5:c.471A= ENSP00000471493.1:p.Thr157=
ENST00000600815.1:c.471A= ENSP00000472936.1:p.Thr157=
NM_001193306.1:c.471A= NP_001180235.1:p.Thr157=
NM_002029.3:c.471A= , LRG_146t1:c.471A= NP_002020.1:p.Thr157=
NM_001193306.2:c.471A= NP_001180235.1:p.Thr157=
NM_002029.4:c.471A= MANE Select NP_002020.1:p.Thr157=